Palmitoylethanolamide

2

Review clinical trials related to Palmitoylethanolamide. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Beneficial Effects of Supplementation With CRONILIEF™ (Palmitoylethanolamide Phospholipids) in Diabetic Subjects With Neuropathic Pain.

This study aims to evaluate the potential benefit of an oral nutritional supplement based on CRONILIEF™ (Palmitoylethanolamide Phospholipids) in diabetic subjects with neuropathic pain, compared to a placebo.

Participants needed: 70
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Azienda di Servizi alla Persona di PaviaUpdated: Feb 17, 2026
Eligibility criteria

Satisfactory metabolic compensation; [+3]

Previous intolerance to a component of the nutraceuticals tested; [+12]

Status: Not yet recruiting

Palmitoylethanolamide vs Ibuprofen for Pain After ESWL

Pain after extracorporeal shock wave lithotripsy (ESWL), a non-surgical procedure used to treat kidney stones, is common and is usually treated with non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. However, NSAIDs may cause side effects in some patients, including stomach irritation and kidney problems. Palmitoylethanolamide (PEA) is a naturally occurring substance in the body with anti-inflammatory and pain-relieving properties and has been shown to be safe in previous studies. This study aims to compare the effectiveness of PEA with ibuprofen for controlling acute postoperative pain after ESWL. Participants undergoing ESWL will be randomly assigned to receive either oral PEA or oral ibuprofen. Pain intensity will be measured using a visual analogue scale during the first 24 hours after the procedure. The use of rescue pain medication and any side effects will also be recorded. The results of this study may help determine whether PEA can be an effective alternative to ibuprofen for the management of acute pain after ESWL.

Participants needed: 120
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Benha UniversityUpdated: Jan 5, 2026Locations: 1
Eligibility criteria

Age 18-65 years [+5]

Chronic pain or daily analgesic use. [+6]